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病毒样颗粒作为一种高效的疫苗平台:多样化的目标和生产系统以及临床开发的进展。

Virus-like particles as a highly efficient vaccine platform: diversity of targets and production systems and advances in clinical development.

机构信息

Fraunhofer USA Center for Molecular Biotechnology, Newark, DE 19711, USA.

出版信息

Vaccine. 2012 Dec 17;31(1):58-83. doi: 10.1016/j.vaccine.2012.10.083. Epub 2012 Nov 6.


DOI:10.1016/j.vaccine.2012.10.083
PMID:23142589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7115575/
Abstract

Virus-like particles (VLPs) are a class of subunit vaccines that differentiate themselves from soluble recombinant antigens by stronger protective immunogenicity associated with the VLP structure. Like parental viruses, VLPs can be either non-enveloped or enveloped, and they can form following expression of one or several viral structural proteins in a recombinant heterologous system. Depending on the complexity of the VLP, it can be produced in either a prokaryotic or eukaryotic expression system using target-encoding recombinant vectors, or in some cases can be assembled in cell-free conditions. To date, a wide variety of VLP-based candidate vaccines targeting various viral, bacterial, parasitic and fungal pathogens, as well as non-infectious diseases, have been produced in different expression systems. Some VLPs have entered clinical development and a few have been licensed and commercialized. This article reviews VLP-based vaccines produced in different systems, their immunogenicity in animal models and their status in clinical development.

摘要

病毒样颗粒(VLPs)是一类亚单位疫苗,它们通过与 VLP 结构相关的更强的保护性免疫原性与可溶性重组抗原区分开来。与亲代病毒一样,VLPs 可以是非包膜的或包膜的,并且可以在重组异源系统中表达一种或几种病毒结构蛋白后形成。根据 VLP 的复杂性,它可以使用目标编码重组载体在原核或真核表达系统中产生,或者在某些情况下可以在无细胞条件下组装。迄今为止,已经在不同的表达系统中生产了针对各种病毒、细菌、寄生虫和真菌病原体以及非传染性疾病的广泛的基于 VLP 的候选疫苗。一些 VLPs 已经进入临床开发阶段,少数已经获得许可并商业化。本文综述了不同系统中生产的基于 VLP 的疫苗,它们在动物模型中的免疫原性及其在临床开发中的状况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ed/7115575/2f0fd6167a38/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ed/7115575/3f9ece838281/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ed/7115575/2f0fd6167a38/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ed/7115575/3f9ece838281/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ed/7115575/2f0fd6167a38/gr2.jpg

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Virus-like particles as a highly efficient vaccine platform: diversity of targets and production systems and advances in clinical development.

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本文引用的文献

[1]
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